Canonical Allele Identifier: CA2710731639

Gene: SQSTM1

Linked Data

• dbSNP Id: rs61480353

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.179833868_179833870dup , CM000667.2:g.179833868_179833870dup	GRCh38
NC_000005.9:g.179260868_179260870dup , CM000667.1:g.179260868_179260870dup	GRCh37
NC_000005.8:g.179193474_179193476dup	NCBI36
NG_011342.1:g.32481_32483dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389805.9:c.1165+86_1165+88dup MANE Select	ENSP00000374455.4:n.1165+86_1165+88dup
ENST00000360718.5:c.913+86_913+88dup	ENSP00000353944.5:n.913+86_913+88dup
ENST00000389805.8:c.1165+86_1165+88dup	ENSP00000374455.4:n.1165+86_1165+88dup
ENST00000510187.5:c.950+641_950+643dup	ENSP00000424477.1:n.950+641_950+643dup
NM_001142298.1:c.913+86_913+88dup	NP_001135770.1:n.913+86_913+88dup
NM_001142299.1:c.913+86_913+88dup	NP_001135771.1:n.913+86_913+88dup
NM_003900.4:c.1165+86_1165+88dup	NP_003891.1:n.1165+86_1165+88dup
XM_017010010.1:c.913+86_913+88dup	XP_016865499.1:n.913+86_913+88dup
NM_003900.5:c.1165+86_1165+88dup MANE Select	NP_003891.1:n.1165+86_1165+88dup
NM_001142298.2:c.913+86_913+88dup	NP_001135770.1:n.913+86_913+88dup
NM_001142299.2:c.913+86_913+88dup	NP_001135771.1:n.913+86_913+88dup